Search results for "Phenotype"

showing 10 items of 1875 documents

Killer toxin-secreting double-stranded RNA mycoviruses in the yeasts Hanseniaspora uvarum and Zygosaccharomyces bailii.

1994

Killer toxin-secreting strains of the yeasts Hanseniaspora uvarum and Zygosaccharomyces bailii were shown to contain linear double-stranded RNAs (dsRNAs) that persist within the cytoplasm of the infected host cell as encapsidated virus-like particles. In both yeasts, L- and M-dsRNAs were associated with 85-kDa major capsid protein, whereas the additional Z-dsRNA (2.8 kb), present only in the wild-type Z. bailii killer strain, was capsid protein, whereas the additional Z-dsRNA (2.8 kb), present only in the wild-type Z. bailii killer strain, was shown to be encapsidated by a 35-kDa coat protein. Although Northern (RNA) blot hybridizations indicated that L-dsRNA from Z. bailii is a LA species,…

Zygosaccharomyces bailiivirusesImmunologySaccharomyces cerevisiaeSaccharomyces cerevisiaeBiologyHanseniasporaTransfectionMicrobiologyPeptide MappingMicrobiologyCapsidVirus-like particleVirologyYeastsRNA VirusesRNA Double-StrandedSequence Homology Amino AcidRNAMycotoxinsbiology.organism_classificationBlotting NorthernYeastPhenotypeCapsidInsect ScienceMycovirusRNA ViralResearch ArticleJournal of virology
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Molecular and morphological patterns of introgression between two large white-headed gull species in a zone of recent secondary contact.

2007

Incomplete reproductive isolation promotes gene flow between diverging taxa. However, any gene encoding for traits involved in the reproductive barriers will be less prone to introgression than neutral markers. Comparing introgression rates among loci is thus informative of the number and functions of loci involved in the reproductive barriers. This study aimed at identifying possible mechanisms of restriction to gene flow across a zone of recent secondary contact between Larus argentatus and Larus cachinnans by comparing introgression patterns for nine microsatellite loci, a fragment of mitochondrial DNA and a set of phenotypic traits. The low linkage disequilibrium between neutral nuclear…

[ SDV.BID ] Life Sciences [q-bio]/BiodiversityGene FlowCharadriiformesSexual Behavior AnimalPhenotypeAnimalsColorHybridization Genetic[SDV.BID]Life Sciences [q-bio]/BiodiversityDNA MitochondrialLinkage Disequilibrium[SDV.BID] Life Sciences [q-bio]/BiodiversityMicrosatellite RepeatsMolecular ecology
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Multidimensionality in host manipulation mimicked by serotonin injection.

2014

Manipulative parasites often alter the phenotype of their hosts along multiple dimensions. ‘Multidimensionality’ in host manipulation could consist in the simultaneous alteration of several physiological pathways independently of one another, or proceed from the disruption of some key physiological parameter, followed by a cascade of effects. We compared multidimensionality in ‘host manipulation’ between two closely related amphipods, Gammarus fossarum and Gammarus pulex, naturally and experimentally infected with Pomphorhynchus laevis (Acanthocephala), respectively. To that end, we calculated in each host–parasite association the effect size of the difference between infected and uninfect…

[ SDV.MP.PAR ] Life Sciences [q-bio]/Microbiology and Parasitology/ParasitologyamphipodsZoologyGeneral Biochemistry Genetics and Molecular BiologyHost-Parasite InteractionsAcanthocephalaPhototaxis[ SDV.EE.IEO ] Life Sciences [q-bio]/Ecology environment/SymbiosisAnimalsAmphipoda[SDV.MP.PAR]Life Sciences [q-bio]/Microbiology and Parasitology/ParasitologymultidimensionalityResearch ArticlesGeneral Environmental ScienceGeneral Immunology and MicrobiologybiologyEcologyHost (biology)General Medicinebiology.organism_classificationAttractionPhenotypeSerotonin Receptor AgonistsserotoninGammarus pulexPulexPhenotypeparasite manipulationPomphorhynchus laevisGeneral Agricultural and Biological SciencesAcanthocephala[SDV.EE.IEO]Life Sciences [q-bio]/Ecology environment/Symbiosis
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Phenotype genotype relationship in human taste

2008

International audience

[CHIM.OTHE] Chemical Sciences/Otherphenotypegenotypehuman taste[CHIM.OTHE]Chemical Sciences/OtherComputingMilieux_MISCELLANEOUS
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PPHD: une plateforme pour le phenotypage a haut debit

2012

International audience; The methodologies for genotyping and high throughput automated platforms for the production of type-omics (genomics, transcriptomics, protected omics ...) have greatly increased over the last few years and are now available to analyze the expression of genes of plants in several environmental conditions. However, a break of conceptual and technical services, non-destructive characterization and dynamic phenotypes, at the organ or plarite, has hundreds of related genotypes (Broadband) remains the limiting factor for the discovery of new characters or new varieties. This systematic exploration of diversity. Genetics within a species or between species requires platform…

[SDE] Environmental Sciences[SDV]Life Sciences [q-bio]phenotypesgenetic analysisgenetic diversity[SDV] Life Sciences [q-bio]crossesgenotypes[SDE]Environmental Sciences[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal Biologygenetic mappingleavestechniquesmutants
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Pois protéagineux : cheminement de la recherche génétique pour la sélection des paramètres à prendre en compte pour l’amélioration de la stabilité du…

2013

Field Pea: development of genetic research for the selection of parameters to take into account to improve yield stability. Legumes were essential in rotations in the past, but they fell off during the 20th century. Maybe they will come back into favour in the 21st century thanks to its economy, agri-environment and food assets. Field Pea is the main crop of this family in France, but it remains underdeveloped because its unstable yield does not enable the farmers to ensure their income security. Therefore researchers should focus on yield stability. Modelling Pea remains difficult because of its indeterminate development. Parameters to take into account are many and their significance must…

[SDE] Environmental Sciencesrootsagroecologyphenotypeélaboration d'idéotypelegumesgenotype[SDV]Life Sciences [q-bio]Genopearesistanceyield stabilitynutrition azotée optimaletolérance au stress hydriqueAphanomyces euteichesphénotypage[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal BiologygeneticsPisum sativumstress tolerancevarietal selectionfabaceaesymbiosisideotype[SDV] Life Sciences [q-bio]acquisition of nitrogen[SDE]Environmental Sciencesstabilité rendementfield peatolérance au froidpois protéagineuxnodulesRhizobium
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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

2017

Subtelomeric 1q43q44 microdeletions cause a syndrome associating intellectual disability, microcephaly, seizures and anomalies of the corpus callosum. Despite several previous studies assessing genotype-phenotype correlations, the contribution of genes located in this region to the specific features of this syndrome remains uncertain. Among those, three genes, AKT3, HNRNPU and ZBTB18 are highly expressed in the brain and point mutations in these genes have been recently identified in children with neurodevelopmental phenotypes. In this study, we report the clinical and molecular data from 17 patients with 1q43q44 microdeletions, four with ZBTB18 mutations and seven with HNRNPU mutations, an…

[SDV.GEN]Life Sciences [q-bio]/GeneticsRepressor Proteins/geneticsddc:618Neurodevelopmental Disorders/geneticsHeterogeneous-Nuclear Ribonucleoproteins/geneticsHeterogeneous-Nuclear RibonucleoproteinsChromosomesRepressor ProteinsPhenotypeChromosomes Human Pair 1Neurodevelopmental DisordersMutationGeneticsPair 1HumansGenetics(clinical)Chromosome Deletion[ SDV.GEN ] Life Sciences [q-bio]/GeneticsOriginal InvestigationHuman
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Assessment of Adult Mouse Brain Neuroanatomical Phenotypes Using Quantitative and Precision Histology

2022

Modelling human neurodevelopmental disorders is important in biomedical research since the brain cannot be easily accessed in humans. In this chapter, we describe a series of standardized procedures for the reliable analysis of neuroanatomical phenotypes (NAPs) of the adult mouse brain using quantitative 2D histological practices. Our goal is to provide the reader an experimental pipeline, ranging from experimental work through to data analysis, which can be performed in any academic research setting with or without access to a histology platform. Depending on the type of sections studied, parasagittal or coronal, the assessment of brain neuroanatomy is performed at stereotaxic sections, at…

[SDV] Life Sciences [q-bio]Mouse models of neurodevelopmental disordersNeuroanatomical phenotypes (NAPs)Ultra-standardized and high-throughput proceduresMouse brain anatomyQuantitative histological analysis
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New insights into the use of rhizobia to mitigate soil N2O emissions

2022

Agriculture is a major anthropogenic source of the greenhouse gas N2O, which is also involved in stratospheric ozone depletion. While the use of rhizobial inoculants has already been reported as an emerging option for mitigating soil N2O emissions, this study presents an in situ abatement of 70% of soil N2O emission using the strain nosZ+ G49 vs. nosZ− USDA138 in association with soybean. Therefore, we consider that the choice of the inoculant strain of a leguminous crop should take into account the capacity of strains to reduce nitrous oxide in addition to their N fixation capacity. This study also clearly suggests that this mitigation option could be considered not only for soybean but al…

[SDV] Life Sciences [q-bio]N<sub>2</sub>O mitigation; rhizobia; legumes; <i>nosZ</i> gene; phenotypes; multiscale approachfood and beveragesPlant Scienceequipment and suppliesAgronomy and Crop ScienceFood Science
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Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an "FCS score".

2018

Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired clearance of triglyceride (TG)-rich lipoproteins from plasma, leading to severe hypertriglyceridaemia (HTG) and a markedly increased risk of acute pancreatitis. It is due to the lack of lipoprotein lipase (LPL) function, resulting from recessive loss of function mutations in the genes coding LPL or its modulators. A large overlap in the phenotype between FCS and multifactorial chylomicronaemia syndrome (MCS) contributes to the inconsistency in how patients are diagnosed and managed worldwide, whereas the incidence of acute hypertriglyceridaemic pancreatitis is more frequent in FCS. A panel of Eu…

[SDV]Life Sciences [q-bio]Diagnosis toolpopulation030204 cardiovascular system & hematologyburdenapoa50302 clinical medicineLoss of Function MutationRisk FactorsChylomicrons030212 general & internal medicineAge of OnsetHypolipidemic AgentsBIOMEDICINA I ZDRAVSTVO. Kliničke medicinske znanosti. Interna medicina.Lipoprotein lipaseplasma triglycerideshyperlipoproteinemiaPrognosis3. Good healthUp-RegulationPhenotypeAcute pancreatitislipids (amino acids peptides and proteins)Hyperlipoproteinemia Type IAcute pancreatitis ; Familial chylomicronaemia syndrome ; Major hypertriglyceridaemia ; Multifactorial chylomicronaemiaCardiology and Cardiovascular MedicineFamilial chylomicronaemia syndromeAlgorithmsacute-pancreatitismedicine.medical_specialtyConsensushypertriglyceridemiaetiologyAcute pancreatitis; Familial chylomicronaemia syndrome; Major hypertriglyceridaemia; Multifactorial chylomicronaemia/Decision Support TechniquesDiagnosis Differential03 medical and health sciencesAcute pancreatitis; Familial chylomicronaemia syndrome; Major hypertriglyceridaemia; Multifactorial chylomicronaemia; Cardiology and Cardiovascular MedicinePredictive Value of TestsInternal medicinemedicineHumansGenetic Predisposition to DiseaseAcute pancreatitiBIOMEDICINE AND HEALTHCARE. Clinical Medical Sciences. Internal Medicine.GenotypingTriglyceridesPregnancyReceiver operating characteristicbusiness.industrysevereMultifactorial chylomicronaemiaReproducibility of Resultsmutationslipoprotein-lipase genemedicine.diseaseConfidence intervalAcute pancreatitisLipoprotein LipasePancreatitisCardiovascular System & CardiologyPancreatitisMajor hypertriglyceridaemiabusinessBiomarkersAtherosclerosis
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